Research workbench
Crystal structure of PI3KALPHA in complex with fragments 7 and 11
Analyse Crystal structure of PI3KALPHA in complex with fragments 7 and 11 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5SW8
- Type
- protein
- Length
- 1,232 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform…
- EC
- 2.7.1.153, 2.7.11.1
- UniProt
- P42336, P27986
- Ligands
- FB1, 70S
- Pockets
- 14 · best druggability 0.86
Structure
x-ray diffraction · 2 distinct chains · 43% helix, 12% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform (EC 2.7.1.153, 2.7.11.1) | protein | 1031 | 39% helix, 14% strand | P42336 |
| B | Phosphatidylinositol 3-kinase regulatory subunit alpha | protein | 201 | 62% helix, 3% strand | P27986 |
Ligands and binding sites
- FB1 · 2-chlorobenzenesulfonamide · ligand · 2 copies · chains A
- 70S · 2H-indazol-5-amine · ligand · chains A
- EPE · 4-(2-hydroxyethyl)-1-piperazine ethanesulfonic acid · additive · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
14 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1194 | 0.86 | 0.87 | 132 | empty |
| 2 | 1055 | 0.84 | 0.85 | 104 | empty |
| 3 | 1019 | 0.84 | 0.85 | 98 | empty |
| 4 | 702 | 0.74 | 0.80 | 71 | empty |
| 5 | 363 | 0.62 | 0.78 | 33 | empty |
Interfaces
1 interface between chains.
- A–B · 2966 Ų buried · 27 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 1 modified (phosphorylation).
Compared structures
- P42336 · AlphaFold monomer V2.0 prediction for phosphatidylinositol 4,5-bisphosphate 3-kinase… · a predicted model of the same protein · chain A against A, TM-score 0.97
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P42336
- Every structure of UniProt P27986
- Elsewhere: RCSB PDB 5SW8 · PDBe 5SW8 · UniProt P42336 · UniProt P27986
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